Canonical Allele Identifier: CA363511401

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32040751-G-C
• MyVariant Identifiers: chr6:g.32008528G>C (hg19) ; chr6:g.32040751G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040751G>C , CM000668.2:g.32040751G>C	GRCh38
NC_000006.11:g.32008528G>C , CM000668.1:g.32008528G>C	GRCh37
NC_000006.10:g.32116507G>C	NCBI36
NG_007941.2:g.7444G>C
NG_008337.2:g.73624C>G
NG_007941.3:g.7447G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1202G>C MANE Select	ENSP00000496625.1:p.Arg401Thr
ENST00000418967.6:c.1202G>C	ENSP00000408860.2:p.Arg401Thr
ENST00000435122.3:c.1112G>C	ENSP00000415043.2:p.Arg371Thr
ENST00000479074.5:n.1343G>C
ENST00000479730.5:n.1318G>C
ENST00000483041.5:n.1371G>C
ENST00000486063.5:n.1181G>C
NM_000500.7:c.1202G>C	NP_000491.4:p.Arg401Thr
NM_001128590.3:c.1112G>C	NP_001122062.3:p.Arg371Thr
XM_011514314.1:c.797G>C	XP_011512616.1:p.Arg266Thr
NM_000500.9:c.1202G>C MANE Select	NP_000491.4:p.Arg401Thr
NM_001368143.1:c.797G>C	NP_001355072.1:p.Arg266Thr
NM_001368144.1:c.797G>C	NP_001355073.1:p.Arg266Thr
NM_001128590.4:c.1112G>C	NP_001122062.3:p.Arg371Thr
NM_001368143.2:c.797G>C	NP_001355072.1:p.Arg266Thr
NM_001368144.2:c.797G>C	NP_001355073.1:p.Arg266Thr